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Open nowFirst seen 5 days ago

Clinical Project Manager

global-channel-management-inc944 open roles

Where
Indianapolis, Indiana, United States
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Your applicationOpen nowClinical Project Managerglobal-channel-management-inc · Indianapolis, Indiana, United States

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  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on global-channel-management-inc's own form.

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The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.3%14 days
  5. 35.6%30 days
  6. 58.1%60 days
This job: first seen 5 days ago

The posting

Clinical Project Manager needs 5+ years experience

Clinical Project Manager requires:

Onsite

Clinical Project management

MS Project, SAP, IMPACT etc.

Clinical Project Manager duties:

Accurately forecast and track direct expenses for clinical budgets Document key team information and clinical decisions in Chorus custom tracking and communication database

Manage clinical operational risks and their impact to the timelines and budgets of clinical studies, including critical path activities

Select and manage external network of vendors to ensure on time and on budget clinical project deliverables

Establish and manage Clinical vendor expectations, performance, and delivery

Serve as the central point of contact for the global clinical team, to resolve clinical implementation issues (internal and external), lead risk assessments and contingency planning, and effective communication across and upward

Partner with regulatory and medical to ensure safety management and monitoring processes are implemented

Provide input into molecule development, clinical regulatory and safety strategy

Manage global cross-functional communication and escalations to ensure alignment on delivery and execution

Utilize clinical operations process knowledge to drive decision making.

Participate in review of clinical database specifications and utilization

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